Gao Guohui, Chen Chong, Yang Yanmei, Yang Han, Wang Jindan, Zheng Yi, Huang Qidi, Hu Xiaoqu
Zhejiang Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Wenzhou Medical College, Wenzhou 325035, Zhejiang, China.
Sheng Wu Gong Cheng Xue Bao. 2012 Aug;28(8):1002-14.
To verify the reliability of targeted detecting HER2 positive cancer cells and clinical pathological tissue specimens with a recombinant anti HER2 single chain antibody in single chain Fv fragment (scFv) format, we have constructed the fusion variable regions of the ScFv specific for HER2/neu. labeled a green-fluorescent protein(GFP). The humanized recombinant Anti HER2 ScFv-GFP gene was inserted into pFast Bac HT A, and expressed in insect cells sf9. Then the recombinant fusion protein Anti HER2 ScFv-GFP was properly purified with Ni2+-NTA affinity chromatography from the infected sf9 cells used to test the specificity of the fusion antibody for HER2 positive cancer cells. Firstly, the purified antibody incubated with HER2 positive breast cancer cells SKBR3, BT474 and HER2 negative breast cancer cells MCF7 for 12 h/24 h/48 h at 37 degrees C, in order to confirm targeted detecting HER2 positive breast cancer cells by Laser Confocal Microscopy. Furthermore, the same clinical pathological tissue samples were assessed by immunohistochemistry (IHC) and the fusion antibody Anti HER2 ScFv-GFP in the meanwhile. The data obtained indicated that the recombinant eukaryotic expression plasmid pFast Bac HT A/Anti HER2 ScFv-GFP was constructed successfully In addition, obvious green fluorescent was observed in insect cells sf9. When the purified fusion antibody was incubated with different cancer cells, much more green fluorescent was observed on the surface of the HER2 positive cancer cells SKBR3 and BT474. In contrast, no green fluorescent on the surface of the HER2 negative cancer cells MCF7 was detected. The concentration of the purified fusion antibody was 115.5 microg/mL, of which protein relative molecular weight was 60 kDa. The analysis showed the purity was about 97% and the titer was about 1:64. The detection results of IHC and fusion antibody testing indicated the conformity. In summary, the study showed that the new fusion antibody Anti HER2 ScFv-GFP can test HER2 positive cancer cells, indicating a potential candidate method for clinical HER2 positive specimens detection.
为验证以单链Fv片段(scFv)形式存在的重组抗HER2单链抗体靶向检测HER2阳性癌细胞及临床病理组织标本的可靠性,我们构建了对HER2/neu特异的ScFv融合可变区,标记绿色荧光蛋白(GFP)。将人源化重组抗HER2 ScFv-GFP基因插入pFast Bac HT A,并在昆虫细胞sf9中表达。然后用Ni2+-NTA亲和层析法从感染的sf9细胞中适当纯化重组融合蛋白抗HER2 ScFv-GFP,用于检测融合抗体对HER2阳性癌细胞的特异性。首先,将纯化后的抗体与HER2阳性乳腺癌细胞SKBR3、BT474及HER2阴性乳腺癌细胞MCF7在37℃下孵育12小时/24小时/48小时,以便通过激光共聚焦显微镜确认对HER2阳性乳腺癌细胞的靶向检测。此外,同时通过免疫组织化学(IHC)和融合抗体抗HER2 ScFv-GFP对相同的临床病理组织样本进行评估。获得的数据表明成功构建了重组真核表达质粒pFast Bac HT A/抗HER2 ScFv-GFP。此外,在昆虫细胞sf9中观察到明显的绿色荧光。当纯化的融合抗体与不同癌细胞孵育时,在HER2阳性癌细胞SKBR3和BT474表面观察到更多绿色荧光。相比之下,在HER2阴性癌细胞MCF7表面未检测到绿色荧光。纯化的融合抗体浓度为115.5μg/mL,其蛋白质相对分子量为60 kDa。分析表明纯度约为97%,效价约为1:64。IHC检测结果与融合抗体检测结果相符。总之,该研究表明新的融合抗体抗HER2 ScFv-GFP可检测HER2阳性癌细胞,为临床HER2阳性标本检测提供了一种潜在的候选方法。